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Case Studies | Pathology | India | Volume 6 Issue 2, February 2017 | Rating: 6.2 / 10
Chromoblastomycosis: An Unusual and Rare Case Report
Reeta Dhar [7] | Deesha Bhemat | Hoogar MB | Atul Jain [3]
Abstract: Chromoblastomycosis is a chronic progressive cutaneous fungal infection caused by several naturally pigmented fungi [1]. It is also known as chromomycosis, cladosporiosis, Fonseca's disease, Pedroso's disease, phaeosporotrichosis, or verrucous dermatitis [2]. The disease was initially considered to be closely related to blastomycosis, which is a different type of a fungal infection caused by dimorphic fungi of the Blastomyces dermatitis sp. It is reflected in the name of the disease, which suggests it is a fungal infection caused by pigmented Blastomyces fungus [3]. In the tissues they form sclerotic cells or muriform cells. Dermal lesions can range from small nodules to large papillary like eruptions [3]. CBM lesions are clinically polymorphic and are commonly misdiagnosed as various other infectious and non-infectious diseases. In its more severe clinical forms, CBM may cause a series of clinical complications, and if not recognized at an early stage, this disease can be refractory to antifungal therapy [4].
Keywords: Chromoblastomycosis, Chromomycosis, Fonseca
Edition: Volume 6 Issue 2, February 2017,
Pages: 2020 - 2021